Men’s Hereditary Cancer Panel – 79 Genes

Understand Your Inherited Cancer Risk Before Symptoms Appear

This comprehensive germline test analyses 79 genes associated with 22 hereditary cancer types, including prostate, colorectal, breast, pancreatic, bladder and gastric cancers.

The results may help you and your healthcare professional plan more personalised screening, prevention and long-term health monitoring.

What the Test Covers

• Prostate cancer risk genes
• Colorectal cancer risk genes
• Pancreatic cancer risk genes
• Bladder cancer risk genes
• Gastric cancer risk genes
• Male breast cancer risk genes
• Other hereditary cancer syndromes

Advanced Genetic Analysis

The panel detects:

• SNVs: Changes affecting a single DNA building block
• Indels: Small DNA insertions or deletions
• Copy-number variants: Missing or duplicated sections of genetic material
• Sanger-verified findings: Pathogenic findings are confirmed using an established verification method

Why Consider This Test?

Certain inherited genetic variants can increase a person’s lifetime risk of developing cancer. These variants may be passed through families, even when there is no obvious history of cancer.

Knowing your inherited risk may support:

• Earlier or more frequent cancer screening
• More personalised prevention planning
• Better-informed healthcare decisions
• Testing recommendations for close family members
• Discussions with a doctor or genetic counsellor

Who Should Consider This Test?

• Men with a personal or family history of cancer
• Men with relatives diagnosed at a young age
• Families affected by several different cancer types
• Men with prostate, colorectal or pancreatic cancer in the family
• Anyone seeking a deeper understanding of inherited cancer risk
• Men interested in more personalised preventive screening

Simple and Convenient

• No fasting required
• Routine blood draw
• Approximately 10–20 minutes at the clinic
• Analysis of 79 genes across 22 hereditary cancer types
• Pathogenic findings verified using Sanger sequencing

Easy E-Voucher Process

1. Purchase your e-voucher.
2. Book at least six hours before visiting through WhatsApp, LINE or email.
3. Visit the MedEx clinic within 180 days of payment.
4. Complete a routine blood draw.
5. Receive your genetic screening report when available.
6. Review significant findings with a qualified healthcare professional or genetic counsellor.

E-Voucher Details

• Validity: 180 days from payment
• Coverage: 79 genes and 22 hereditary cancer types
• Sample: Blood
• Clinic time: Approximately 10–20 minutes
• Fasting: Not required
• Booking: At least six hours in advance
• Booking channels: WhatsApp, LINE or email

Purchase your e-voucher today and take a proactive step towards understanding your inherited cancer risk.

This test assesses inherited cancer risk; it does not diagnose cancer. A positive result does not mean cancer will develop, while a negative result does not eliminate all cancer risk. Results should be reviewed with a qualified healthcare professional or genetic counsellor.